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Oxa-48 in complex with compound 12A

Analyse Oxa-48 in complex with compound 12A in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5QAI
Type
protein
Length
968 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-lactamase
EC
3.5.2.6
UniProt
Q6XEC0
Ligands
VM7, CL
Pockets
8 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 41% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DBeta-lactamase (EC 3.5.2.6)protein24241% helix, 21% strandQ6XEC0

Ligands and binding sites

  • VM7 · 3-(3-methylsulfonylphenyl)benzoic acid · ligand · 4 copies · chains A, B, C, D
  • CL · Chloride ion · ion · 2 copies · chains A, D
  • EDO · 1,2-ethanediol · additive · 9 copies · chains A, B, C, D
  • DMS · Dimethyl sulfoxide · additive · chains A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110350.780.8096empty
29230.760.7997VM7, EDO
32150.530.7729empty
41010.370.7521VM7
51090.360.7321VM7

Interfaces

5 interfaces between chains.

  • A–B · 453 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 419 Ų buried · 7 hydrogen bonds · protein-protein
  • C–D · 294 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 268 Ų buried · 4 hydrogen bonds · protein-protein
  • B–D · 22 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (carboxylation).

Compared structures

  • 5QAI · OXA-48 IN COMPLEX WITH COMPOUND 12a · the same entry in another collection · chain A against A, TM-score 1.00

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